Swati Banerjee

1.2k total citations
27 papers, 905 citations indexed

About

Swati Banerjee is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Swati Banerjee has authored 27 papers receiving a total of 905 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cellular and Molecular Neuroscience, 12 papers in Molecular Biology and 12 papers in Cell Biology. Recurrent topics in Swati Banerjee's work include Neurobiology and Insect Physiology Research (14 papers), Cellular transport and secretion (7 papers) and Axon Guidance and Neuronal Signaling (5 papers). Swati Banerjee is often cited by papers focused on Neurobiology and Insect Physiology Research (14 papers), Cellular transport and secretion (7 papers) and Axon Guidance and Neuronal Signaling (5 papers). Swati Banerjee collaborates with scholars based in United States, Russia and China. Swati Banerjee's co-authors include Manzoor A. Bhat, Aurea D. Sousa, Raehum Paik, Jingjun Li, Anilkumar M. Pillai, Stephen L. Rogers, Zhiguo Liang, Sarah Paul, Victoria Wu and Greg J. Beitel and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and Genes & Development.

In The Last Decade

Swati Banerjee

26 papers receiving 888 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Swati Banerjee United States 14 462 387 245 127 122 27 905
Mark Eddison United States 15 696 1.5× 365 0.9× 186 0.8× 106 0.8× 67 0.5× 24 1.3k
Jaeda Coutinho‐Budd United States 11 548 1.2× 354 0.9× 289 1.2× 147 1.2× 63 0.5× 20 1.0k
Nina Offenhäuser Italy 13 730 1.6× 393 1.0× 268 1.1× 114 0.9× 92 0.8× 19 1.4k
Katarína Tiklová Sweden 14 753 1.6× 395 1.0× 162 0.7× 69 0.5× 201 1.6× 20 1.1k
Junhai Han China 20 483 1.0× 506 1.3× 163 0.7× 195 1.5× 85 0.7× 59 1.1k
Andrew W. Custer United States 9 416 0.9× 325 0.8× 197 0.8× 168 1.3× 45 0.4× 9 852
Samuel Sidi United States 15 1.0k 2.2× 248 0.6× 357 1.5× 106 0.8× 85 0.7× 24 1.5k
Martin M. Riccomagno United States 9 648 1.4× 223 0.6× 147 0.6× 125 1.0× 47 0.4× 19 1.0k
Sean M. Buchanan United States 13 552 1.2× 210 0.5× 103 0.4× 173 1.4× 102 0.8× 15 1.1k
Julia A. Kaltschmidt United States 19 907 2.0× 484 1.3× 657 2.7× 106 0.8× 62 0.5× 35 1.6k

Countries citing papers authored by Swati Banerjee

Since Specialization
Citations

This map shows the geographic impact of Swati Banerjee's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Swati Banerjee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Swati Banerjee more than expected).

Fields of papers citing papers by Swati Banerjee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Swati Banerjee. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Swati Banerjee. The network helps show where Swati Banerjee may publish in the future.

Co-authorship network of co-authors of Swati Banerjee

This figure shows the co-authorship network connecting the top 25 collaborators of Swati Banerjee. A scholar is included among the top collaborators of Swati Banerjee based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Swati Banerjee. Swati Banerjee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Shi, Qian, et al.. (2025). Tubulin Polymerization Promoting Proteins: Functional Diversity With Implications in Neurological Disorders. Journal of Neuroscience Research. 103(5). e70044–e70044. 1 indexed citations
2.
Banerjee, Swati & Viktor Jirsa. (2024). A review of epileptic markers: from ion channels, astrocytes, synaptic imbalance to whole brain network dynamics. SHILAP Revista de lepidopterología. 3(5). 478–492. 3 indexed citations
3.
Chen, Shuting, Yong Lin, Jing Xie, et al.. (2022). Drosophila Homolog of the Human Carpenter Syndrome Linked Gene, MEGF8, Is Required for Synapse Development and Function. Journal of Neuroscience. 42(37). 7016–7030. 2 indexed citations
4.
Xie, Jing, Shuting Chen, Jean C. Bopassa, & Swati Banerjee. (2021). Drosophila tubulin polymerization promoting protein mutants reveal pathological correlates relevant to human Parkinson’s disease. Scientific Reports. 11(1). 13614–13614. 9 indexed citations
5.
Paik, Raehum, Swati Banerjee, Anilkumar M. Pillai, Manzoor A. Bhat, & Jingjun Li. (2021). Axonal Ensheathment and Septate Junction Formation in the Peripheral Nervous System of Drosophila. UNC Libraries. 1 indexed citations
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Bhushan, Bharat, Laura Molina, Kelly Koral, et al.. (2020). Yes‐Associated Protein Is Crucial for Constitutive Androstane Receptor‐Driven Hepatocyte Proliferation But Not for Induction of Drug Metabolism Genes in Mice. Hepatology. 73(5). 2005–2022. 15 indexed citations
8.
Matamoros, Andrew J., Calvin H. Jan, Qin Wang, et al.. (2020). The microtubule regulator ringer functions downstream from the RNA repair/splicing pathway to promote axon regeneration. Genes & Development. 34(3-4). 194–208. 11 indexed citations
9.
Shi, Qian, Yong Lin, Afaf Saliba, et al.. (2019). Tubulin Polymerization Promoting Protein, Ringmaker, and MAP1B Homolog Futsch Coordinate Microtubule Organization and Synaptic Growth. Frontiers in Cellular Neuroscience. 13. 192–192. 13 indexed citations
10.
Banerjee, Swati, et al.. (2016). Neurexin, Neuroligin and Wishful Thinking coordinate synaptic cytoarchitecture and growth at neuromuscular junctions. Molecular and Cellular Neuroscience. 78. 9–24. 32 indexed citations
11.
Banerjee, Swati, et al.. (2014). Genetic aspects of autism spectrum disorders: insights from animal models. Frontiers in Cellular Neuroscience. 8. 58–58. 112 indexed citations
12.
Chen, Yu‐Chi, Yong Lin, Swati Banerjee, et al.. (2012). DrosophilaNeuroligin 2 is Required Presynaptically and Postsynaptically for Proper Synaptic Differentiation and Synaptic Transmission. Journal of Neuroscience. 32(45). 16018–16030. 55 indexed citations
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Banerjee, Swati, et al.. (2010). Drosophila Neurexin IV Interacts with Roundabout and Is Required for Repulsive Midline Axon Guidance. Journal of Neuroscience. 30(16). 5653–5667. 31 indexed citations
16.
Banerjee, Swati, Roland J. Bainton, Nasima Mayer, Robert B. Beckstead, & Manzoor A. Bhat. (2008). Septate junctions are required for ommatidial integrity and blood–eye barrier function in Drosophila. Developmental Biology. 317(2). 585–599. 28 indexed citations
17.
Banerjee, Swati & Manzoor A. Bhat. (2007). Glial ensheathment of peripheral axons in Drosophila. Journal of Neuroscience Research. 86(6). 1189–1198. 27 indexed citations
18.
Banerjee, Swati, Anilkumar M. Pillai, Raehum Paik, Jingjun Li, & Manzoor A. Bhat. (2006). Axonal Ensheathment and Septate Junction Formation in the Peripheral Nervous System ofDrosophila. Journal of Neuroscience. 26(12). 3319–3329. 93 indexed citations
19.
Banerjee, Swati, Aurea D. Sousa, & Manzoor A. Bhat. (2006). Organization and Function of Septate Junctions: An Evolutionary Perspective. Cell Biochemistry and Biophysics. 46(1). 65–78. 111 indexed citations
20.
Agrawal, Namita, et al.. (2001). Spatial regulation of DELTA expression mediates NOTCH signalling for segmentation of Drosophila legs. Mechanisms of Development. 105(1-2). 115–127. 19 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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